Kinetic energy photodetachment photoelectron

ZEKE (zero kinetic energy) photoelectron spectroscopy has also been applied to negative ions [M]. In ZEKE work, the laser wavelengdi is swept tlirough photodetachment thresholds and only electrons with near-zero kinetic energy are... 

Following the above-mentioned spectroscopic study by Johnson and co-workers [55], Neumark and co-workers [56] explored the ultrafast real-time dynamics that occur after excitation into the CTTS precursor states of I (water) [n — 4-6) by applying a recently developed novel method with ultimate time resolution, i.e., femtosecond photoelectron spectroscopy (FPES). In anion FPES, a size-selected anion is electronically excited with a femtosecond laser pulse (the pump), and a second femtosecond laser pulse (the probe) induces photodetachment of the excess electron, the kinetic energy of which is determined. The time-ordered series of the resultant PE spectra represents the time evolution of the anion excited state projected on to the neutral ground state. In the study of 1 -(water), 263 nm (4.71 eV) and 790 nm (1.57 eV) pulses of 100 fs duration were used as pump and probe pulses, respectively. The pump pulse is resonant with the CTTS bands for all the clusters examined. 

A more powerful experimental technique to probe the electronic structure of transition-metal clusters is size-selected anion photoelectron spectroscopy (PES) [70. 71. 72. 73. 74. 75 and 76]. In PES experiments, a size-selected anion cluster is photodetached by a fixed wavelength photon and the kinetic energies of the photoemitted electrons are measured. PES experiments provide direct measure of the electron affinity and electronic energy levels of neutral clusters. This technique has been used to study many types of clusters over a large cluster size range and can probe how the electronic structures of transition-metal clusters evolve from molecular to bulk [77. 78. 79, 80 and M] Research has focused on the 3d transition-metal clusters, for which there have also been many theoretical studies [82, M, M, 86, M and 89]. It is found that the electronic structure of the small transition-metal clusters is molecular in nature, with discrete electronic states. However, the electronic structure of the transition-metal clusters approaches that of the bulk rapidly. Figure Cl. 14 shows that the electronic structure of vanadium clusters with 65 atoms is already very similar to that of bulk vanadium [90]. Other 3d transition-metal clusters also show bulk-like electronic structures in similar size range [78]. 

Abbreviations used in the tables calc = calculated value PT = photodetachment threshold using a lamp as a light source LPT = laser photodetachment threshold LPES = laser photoelectron spectroscopy DA = dissociative attachment attach = electron at-tachment/detachment equilibrium e-scat = electron scattering kinetic = dissociation kinetics Knud=Knudsen cell CT = charge transfer CD = collisional detachment and ZEKE = zero electron kinetic energy spectroscopy. 

There have been numerous photodetachment studies of small cluster anions, and we now give some examples. Noble metal clusters (Cu, Ag,7, Au , n = 1-10) have been studied by Ho et al. [23], who resolved vibrations in all three dimers. Studies of alkali metal cluster anions have included those of Na ( = 2-5), K (n = 2-19), RbJ 3, and CS2-3 [24,25]. Carbon cluster anions C,T have photoelectron spectra that are consistent with linear chains for n = 2-9 and monocyclic rings for n = 10-29 [26]. Photoelectron spectra of Sb and Bi to n = 4 [27] show rich vibrational structure for the dimers, and the spectra of the larger clusters could be interpreted in terms of ab initio calculations. The threshold photodetachment (zero electron kinetic energy, ZEKE) spectrum of Si4 [28] shows a progression of well-resolved transitions between the ground state of the rhombic anion (Dzh, and vibrational levels of the first excited... 

Figure 9 Anion photoelectron spectroscopy. Its unique features are (I) Intrinsic mass selectivity and (ii) neutrals as final states. Here, as an example the results for compounds of iron, carbon and hydrogen are shown which exist in catalytic processes, high-temperature terrestrial or low-temperature astrophysical chemistry. Bottom spectrum a primary anion mass spectrum containing anions of the complexes of interest. Top spectra anion photoelectron spectra obtained by electron kinetic energy analysis after laser-induced photodetachment. They reveal the change of molecular structure and electronic energies for increasing numbers of hydrogen atoms in the complex.

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